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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172495Generated: November 2, 2026

Furfurylamine → HCID 131728466, compound

https://huagongshe.com/reaction/1172495

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFurfurylamineHCID 3438—
Reactant4-Chloro-2-(2-chloro-ethylamino)-6-methyl-10,10-dioxo-10,11-dihydro-5-oxa-10lambda*6*-thia-dibenzo[a,d]-cycloheptene-8-carboxylic acid methyl esterHCID 131728446—
CatalystTetrabutylammonium IodideHCID 67553—
SolventMethanolHCID 887—
ProductHCID 131728466HCID 131728466—

Reaction Conditions

Temperature110 °C

Reaction Steps

Freshly distilled furfurylamine (0.58 g, 0.60 mmol) and tetrabutylammonium iodide (0.010 g, 0.027 mmol) were sequentially added with stirring to a solution of Example 56k (0.5 g, 1.20 mmol) in dry methanol (10 mL). The reaction mixture was stirred at 110° C. for 5 h in an atmosphere of nitrogen. It was concentrated, treated with methanolic HCl solution (15 mL), refluxed overnight, concentrated, treated with water and extracted with ethyl acetate. The organic layer was washed with water, brine, dried and purified using flash chromatography (silica gel, methanol/chloroform) to obtain the title compound as a white solid. Yield: 0.438 g, (84.88%); 1H NMR (DMSO-d6): δ 1.70 (s, 2H, CH2), 2.30 (m, 6H, 3CH2), 2.65 (s, 3H, CH3), 3.05 (q, 2H, CH2), 3.60 (t, 2H, CH2), 3.90 (s, 3H, OCH3), 5.10 (s, 2H, CH2), 6.25 (t, 1H, NH), 6.70 (s, 1H, Ar), 6.70 (s, 1H, Ar), 8.10 (s, 1H, Ar), 8.15 (s, 1H, Ar); MS (CI+): m/e (ES+) 490 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834001B2
Source datasetuspto-grants-2010_11
ORD IDord-8ca7f2cf349741bba6d9a31ea5cdd466
Source noteuspto-grants-2010_11